drugset / Trial / NCT00123942

Trial of MEDI-507 in CD2-Positive Lymphoproliferative Disease

NCT00123942 ↗

Phase 1 Terminated 31 enrolled MedImmune LLC
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The primary objective of this study is to determine the maximum tolerated dose (MTD) and safety and tolerability of MEDI-507 in patients with CD2-positive lymphoproliferative disorders.

Timeline

Start
2004-04
Primary completion
—
Completion
—

Outcome

Outcome not reported

Stopped: “After review of safety events and have decided that further dose escalation of MEDI-507 as a single agent is not feasible.”

Drugs

EvaluationDrugModalityDoseRoute
Subject MEDI-507 Monoclonal antibody — —